Thomas Lücke - Concepedia

Author

Thomas Lücke

Also Known As

Alice Kuster, Angela M. Kaindl, Claudia Maria Denkinger, Gereon Heuft, Helmke, Knut, Hermann Kalhoff, Johannes Peter Haas, Katharina Hecker, Lucke, Thomas, Lücke, Thomas

700

Publications

5.7K

Citations

H-Index

272

Concepts

All Affiliations

Medizinische Hochschule Hannover Ruhr University Bochum University Hospitals of the Ruhr-University of Bochum St. Josef-Hospital Ludwig-Maximilians-Universität München

About

Thomas Lücke is an author at Medizinische Hochschule Hannover specializing in medicine, pediatrics, and neurology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	29	55	2.3K
2	Health Sciences	13	13	508
3	Engineering	4	4	278
4	Education	3	3	117
5	Arts	1	1	13

Thomas Lücke

117

Publications

4.8K

Citations

H-Index

Page 1

	Year	Citations
Continuous monitoring of regional cerebral blood flow: experimental and clinical validation of a novel thermal diffusion microprobe Peter Vajkoczy, Harry Roth, Péter Horn, Journal of neurosurgery	2000	229
N-methyl-D-aspartate (NMDA) and non-NMDA receptor antagonists block the hyperexcitability of dorsal horn neurons during development of acute arthritis in rat's knee joint Volker Neugebauer, Thomas Lücke, Hans-Georg Schaible Journal of Neurophysiology Pain MedicineSpecific NmdaNeuropathic PainAnesthetic MechanismMolecular Pain	1993	192
Use of guidelines improves the neurological outcome in glutaric aciduria type I Jana Herınger, S. P. Nikolas Boy, Regina Ensenauer, Annals of Neurology	2010	168
Requirement of Metabotropic Glutamate Receptors for the Generation of Inflammation‐evoked Hyperexcitability in Rat Spinal Cord Neurons Volker Neugebauer, Thomas Lücke, Hans‐Georg Schaible European Journal of Neuroscience	1994	159
CLPB Mutations Cause 3-Methylglutaconic Aciduria, Progressive Brain Atrophy, Intellectual Disability, Congenital Neutropenia, Cataracts, Movement Disorder Saskia B. Wortmann, Szymon Ziętkiewicz, Maria Kousi, The American Journal of Human Genetics Genetic DisorderGeneticsProgressive Brain AtrophyPathologyCongenital Neutropenia	2015	135
Molecular characterization of folate receptor 1 mutations delineates cerebral folate transport deficiency Marcel Grapp, Isabell Anna Just, Tarja Linnankivi, Brain Brain DevelopmentGeneticsDisease Gene IdentificationSocial SciencesClinical Genetics	2012	126
Occurrence and fate of amisulpride, sulpiride, and lamotrigine in municipal wastewater treatment plants with biological treatment and ozonation Anna Bollmann, Wolfram Seitz, Carsten Prasse, Journal of Hazardous Materials Chemical EngineeringEngineeringEffluent DisposalEnvironmental EngineeringBioremediation	2016	122
Antibodies to MOG and AQP4 in children with neuromyelitis optica and limited forms of the disease Christian Lechner, Matthias Baumann, Eva-Maria Hennes, Journal of Neurology Neurosurgery & Psychiatry	2015	117
Decline of Acute Encephalopathic Crises in Children with Glutaryl-CoA Dehydrogenase Deficiency Identified by Newborn Screening in Germany Stefan Kölker, Sven F. Garbade, Nikolas Boy, Pediatric Research Acute Encephalopathic CrisesNewborn ScreeningNeonatologyPediatric HydrocephalusPediatric Hematology	2007	111
Fabry disease: reduced activities of respiratory chain enzymes with decreased levels of energy-rich phosphates in fibroblasts Thomas Lücke Molecular Genetics and Metabolism Energy-rich PhosphatesFibrosisFabry DiseaseCellular EnzymologyMitochondrial Function	2004	100

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